ZMP
trpm5
Ensembl ID:
ZFIN ID:
Description:
transient receptor potential cation channel subfamily M member 5 [Source:RefSeq peptide;Acc:NP_0011
Human Orthologue:
TRPM5
Human Description:
transient receptor potential cation channel, subfamily M, member 5 [Source:HGNC Symbol;Acc:14323]
Mouse Orthologue:
Trpm5
Mouse Description:
transient receptor potential cation channel, subfamily M, member 5 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34168 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17123 | Essential Splice Site | Available for shipment | Available now |
sa10868 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34168
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083473 | Nonsense | 490 | 1160 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 50141644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48411880 |
GRCz11 | 7 | 48684656 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAAAAGGCAGACTTTTCCACAGCCAGAAAAACCTTCCAGACATGGAC[A/T]GACGATGTGAGCACCCTTGGAGAGACCTCTTCCTTTGGGCTATTCTGCAG
Long Flanking Sequence:
ACACAGTGTGTGATCTGTGACGCCTCACATAGATAAACTGTGAACGTCCAGAAAGATAGGATTTAAACCAACTTAACATGTTTCCATTTACACCAGAATGTGCAATAAATAGTATAGAAAAATATTTGGCCAATATACAATAATTACAAATTCTGGAATCTGAGGGTTAAAAAAGTCTAAATACTGAAAAATTGGCTTTAATGTTGGACAAATCAAGTTCTTAGTGATGCGTATTATGAATCAAAAATGTAATTTTGAAATTTACAAAATATCTTCATGGAACGTGATCTTTACTTAATATTCAAATGATTTTTAGCCATAAAAGAAAAACCAATCACTTTGCCCCATGCAAACTCTATTTGACTTTTGCTAAAAATATGCTCATACAATGTAAGATTTAGTTTTTGTGGTCCAGAGTCACATATTACATGTATTTATTTCAGGAAAGGATGGGAAAAGGCAGACTTTTCCACAGCCAGAAAAACCTTCCAGACATGGAC[A/T]GACGATGTGAGCACCCTTGGAGAGACCTCTTCCTTTGGGCTATTCTGCAGAATAGGCAGGAAATGGCAAACTACTTCTGGGCCATGGTGGGGGTTTTTTCATATTCATAAACCAAGTCAATTTACATGTTCCCAAATGGTTTTTTAGACCTTATAAAAAGAGGTGCTTTAATTTATCACCAATCATTTTCAACTATCACAAATGACCTCAGCATTGTTTAAAGATCAAACTTTATATGGGTCAGTGAGCCAAGAACAATTTGTGTGAACAAAACTGCTGAGAAGCTAAGAGTCAATATTAAATGCTTAAGGCATTCTTGTGGTACACGCTTGTGCATATTTTAGTACAATGCATTATTGTACATCAGTGTTTAATAACCCTTTGTGTGTTTTAGGGCCCGGAGGCAGTGGCAGCTGCTCTGGTGGGCTGTAAGATCATGAAGGAGATGGCCCATCTGGCTACTGAAGCGGAGTCTGCTCGCAGTATGAAGAATGCCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17123
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083473 | Essential Splice Site | 965 | 1160 | 20 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 50154339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48424575 |
GRCz11 | 7 | 48697351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTMATTAAAAAAGGAAAATGTAACTAATCATCTTGTCACCCCTCTTCAC[A/G]GCTACACRTTYCAAGTGGTGCAGGAGAATGCAGATATCTTCTGGAAGTTT
Long Flanking Sequence:
CATGTTATATGGAATCCATTTATTGAGTACTTTAACAAAAGACCAGTGATTGAACGCTGATTGAAACACCTCAAATCCCCCCAATTTAATTGTTTTTTTCTTTCTTTTGCTCTTTCCCCCACTCTTCTCTGTTTTTTTTTATTTTTATTCATATATTAACATGATGTTAACTTTTTGTTTAAAAGAAAAAAAAGTATACATAAAGTTATAATTTGTACTCATGTCAAAATACAATAAAGAAAATGTTTAACATGCAGTACCACTCTATACTGTAGGTTTTCAAGATTAATTTGACATTAGGCAAAATGAGCATGATACATCCCCTTTAACGTTTTTTTATCTGAAACATTATTCCAGGGGGTGTGTTTATGTAAAATTGAGCAGTTTGGATCAAGGAAGAAGTCTCATTGCACTCTAACAAAAATGTGAAATCACAAGCAATCATATACCTTTCATTAAAAAAGGAAAATGTAACTAATCATCTTGTCACCCCTCTTCAC[A/G]GCTACACGTTCCAAGTGGTGCAGGAGAATGCAGATATCTTCTGGAAGTTTCAGCGCTACAACTTAATTGTTGAATACCACAGCCGCCCGGCACTAGCACCACCTTTCATCATCATCAGCCACATCACACAGGCTCTCCTCAGCTTCATCAAAAAGACAGAAAACACACAGGATCTGCTGGGCAAGTAGACTTTACACTGCCTGAGCACTTCTCTGTTAGATTTTATATATATATATATATATATATATATATATATATATATATATATATAGTTCATCATGCAGAGCTATTTTTCATATTGTTTTCACAAGAACTCAATGATAAGTGAGGTCAATTAAGGACACGTGGCAGGTAAAGCAAATGTGATATTTAAAGAAACAGCGTCAAATCTTAGTTCCTCTTTTGTTGTTGTGGTGGATAGAGAGGGAACTGCCGTCTGGCCTGGACCAGAAGCTCATGACATGGGAGACGGTGCAGAAAGAGAACTATCTGGCTAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10868
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083473 | Nonsense | 1050 | 1160 | 21 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 50154835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48425071 |
GRCz11 | 7 | 48697847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCAGAAGCTCATGACATGGGAGACGGTGCAGAAAGAGMACTATCTGGCT[A/T]AACTGGAGCATGAGCACAGAGAGAGCAGCGGAGAGAGACTCAGATACACT
Long Flanking Sequence:
TCACAGCTACACGTTCCAAGTGGTGCAGGAGAATGCAGATATCTTCTGGAAGTTTCAGCGCTACAACTTAATTGTTGAATACCACAGCCGCCCGGCACTAGCACCACCTTTCATCATCATCAGCCACATCACACAGGCTCTCCTCAGCTTCATCAAAAAGACAGAAAACACACAGGATCTGCTGGGCAAGTAGACTTTACACTGCCTGAGCACTTCTCTGTTAGATTTTATATATATATATATATATATATATATATATATATATATATATATATAGTTCATCATGCAGAGCTATTTTTCATATTGTTTTCACAAGAACTCAATGATAAGTGAGGTCAATTAAGGACACGTGGCAGGTAAAGCAAATGTGATATTTAAAGAAACAGCGTCAAATCTTAGTTCCTCTTTTGTTGTTGTGGTGGATAGAGAGGGAACTGCCGTCTGGCCTGGACCAGAAGCTCATGACATGGGAGACGGTGCAGAAAGAGAACTATCTGGCT[A/T]AACTGGAGCATGAGCACAGAGAGAGCAGCGGAGAGAGACTCAGATACACTTCCTCAAAGTGAGTAATGCTGCACTCATATGAGATGAATTAATACCCATCTTAGTTTATGTTGAGGTTTGTTTCATGAGTATTAAGTCCAAATCCATGCGAATGACTGCATGTGTATCCGCTTTTAACCTATTTTTGGTGTGTTGCTTAGGGTACAGACTTTGCTGAGGATGGTTGGGGGTTTTAAGGACCAAGAAAAGCGAATGGCAACAGTGGAGACTGAGGTGAAGAGAAATAGTTGATCTTAATGATAATTATATTAATGGAGATAAATAATAAAACAGTTCTACATTTTAAACAATAGCAGAGTTCACAGTCACACTGTTATTATAACAATTATGGCACAGAGGAACAATACAGATAAAATCACTCATAACTCATTTAATATGTATTGTTTTTTGTCCTTGTTCTGGATCCATTTTCAACCTAAAGGATTGTTATTATATAAAAT
Associated Phenotype:
Not determined